Mutation saturation for fitness effects at human CpG sites
Whole exome sequences have now been collected for millions of humans, with the related goals of identifying pathogenic mutations in patients and establishing reference repositories of data from unaffected individuals. As a result, we are approaching an important limit, in which datasets are large en...
| Hauptverfasser: | , |
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| Format: | Artikel |
| Sprache: | English |
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eLife Sciences Publications Ltd
2021-11-01
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| Schriftenreihe: | eLife |
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| Online Zugang: | https://elifesciences.org/articles/71513 |